
CRISPR knockout cell lines are engineered through targeted genome editing to eliminate gene function, supporting studies of cellular biology, disease mechanisms, and drug discovery.
SIRT1 (sirtuin 1) encodes a member of the class I sirtuin family of NAD+-dependent regulatory proteins. SIRT1 contains a conserved sirtuin catalytic domain and has been implicated in regulation of intracellular signaling, chromatin-associated processes, and protein modification through deacetylation and related activities. Through its ability to modify regulatory proteins and chromatin-associated factors, SIRT1 can influence gene expression and cellular responses to metabolic and environmental conditions.
A human breast cancer model, SUM-149PT was established from a primary inflammatory breast carcinoma of a 55-year-old female. The cells are classified as a human breast cancer cell line and represent a model of inflammatory breast cancer. SUM-149PT carries documented BRCA1 and TP53 alterations and has been extensively characterized by genomic and transcriptomic analyses.
Comprehensive quality control includes STR authentication, sterility testing (bacteria and fungi), and mycoplasma screening to ensure purity and performance. Genotype is confirmed by two rounds of PCR and Sanger sequencing, and complete validation reports are provided for make-to-order products.

Cas9 cell lines in our cell bank can stably express Cas9 protein. Each Cas9 Stable Cell Line is easy to use and enables gene knockout simply by transfecting gRNA, while transfection of gRNA and donor DNA results in gene knock-in or point mutations
These Cas9 stable cell lines have been used to construct the KO cell lines for various genes, gene KO efficiency 5-10 times improved.
Selected cells, low passages, good cell condition, high activity, applicable for all kinds of gene-editing experiments.
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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